KT-253
A Phase 1, Multicenter, Open-Label, Dose-Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Clinical Activity of Intravenously Administered KT-253 in Adult Patients With High Grade Myeloid Malignancies and Acute Lymphocytic Leukemia, Lymphoma and Advanced Solid Tumors
Arms / Cohorts
Experimental, Phase 1 Dose Escalation:Arm A: Solid Tumors and Lymphomas
Accepting patients
Experimental, Phase 1 Dose Escalation:Arm B: High Grade Myeloid Malignancies and ALL
Accepting patients
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